Dual-Stimuli-Responsive Nanoassemblies as Tunable Releasing Carriers

被引:50
|
作者
Kang, Yang [1 ]
Ma, Yuan [1 ]
Zhang, Sheng [2 ]
Ding, Li-Sheng [1 ]
Li, Bang-Jing [1 ]
机构
[1] Chinese Acad Sci, Chengdu Inst Biol, Key Lab Mt Ecol Restorat & Bioresource Utilizat, Chengdu 610041, Peoples R China
[2] Sichuan Univ, Polymer Res Inst, State Key Lab Polymer Mat Engn, Chengdu 610065, Peoples R China
基金
中国国家自然科学基金;
关键词
POLYMERIC MICELLES; BETA-CYCLODEXTRIN; BLOCK; COPOLYMER; WATER; NANOPARTICLES; NONCOVALENT; TRANSITION; VESICLES; DRIVEN;
D O I
10.1021/acsmacrolett.5b00171
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Two end-decorated homopolyrners, methoxy polyethylene glycol-ferrocene (mPEG-Fc) and poly(N-isopropylacrylamide)-beta-cyclodextrin (PNIPAM-beta-CD), were further orthogonally self-assembled into stable micelles in aqueous solution by controlling the temperature of the solution via terminal host-guest interactions. Because of the H2O2 cleavable CD/Fc connection and thermoresponsive PNIPAM, an H2O2 and thermo dual-controlled drug release based on this system was also achieved. Interestingly, the cytotoxicity evaluation of mPEG-Fc/PNIPAM-beta-CD indicated good biocompatibility. Compared with free doxorubicin, the doxorubicin-loaded supramolecular micelles exhibited equal cellular proliferation inhibition toward A549 cells. This supramolecular complex is thus anticipated to serve as a promising new type of alternative drug-delivery system.
引用
收藏
页码:543 / 547
页数:5
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